The following data is part of a premarket notification filed by Vident with the FDA for Vita Zeta Crown And Bridge Acrylic Veneering System.
Device ID | K961434 |
510k Number | K961434 |
Device Name: | VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM |
Classification | Material, Tooth Shade, Resin |
Applicant | VIDENT 3150 EAST BIRCH ST. Brea, CA 92821 |
Contact | Ray E Morrow |
Correspondent | Ray E Morrow VIDENT 3150 EAST BIRCH ST. Brea, CA 92821 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-04-15 |
Decision Date | 1996-07-08 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
J017CVLCPBKSC0 | K961434 | 000 |
J017CVLCCBK0 | K961434 | 000 |
J017C4450130 | K961434 | 000 |
J017CVLCPTKA30 | K961434 | 000 |
J017CVLCPTK2M20 | K961434 | 000 |
J017CVLCFTK2M20 | K961434 | 000 |
J017CVLCFBKSV10 | K961434 | 000 |
J017CVLCCTKA30 | K961434 | 000 |
J017CVLCCTK2M20 | K961434 | 000 |
J017CVLCCBKC0 | K961434 | 000 |
J017CVLCCBKS0 | K961434 | 000 |
J017CVLCPBKS0 | K961434 | 000 |
J017CVLCPBKC0 | K961434 | 000 |
J017CVLCPBK0 | K961434 | 000 |
J017CVLCFPKV10 | K961434 | 000 |
J017CVLCFCKV10 | K961434 | 000 |
J017CVLCFBKSCV20 | K961434 | 000 |
J017CVLCFBKCV20 | K961434 | 000 |
J017CVLCCBKSC0 | K961434 | 000 |
J017C44433F40 | K961434 | 000 |